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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352701Generated: November 1, 2026

Sodium Cyanide → HCID 69430029, compound

https://huagongshe.com/reaction/1352701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 19963213HCID 19963213—
SolventDimethylformamideHCID 6228—
ProductHCID 69430029HCID 6943002948.2%

Reaction Steps

A solution of 38.1 g (117 mmol) of (7SR,9aSR)-7-(methanesulfonyloxy)methyl-2-(pyrimidin-2-yl)-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido[1,2-a]pyrazine (prepared according to U.S. Pat. No. 5,122,525) and 6.01 g (122 mmol) of sodium cyanide in 500 mL of dry DMF was heated at 110° C. for 16 h. The mixture was cooled to room temperature, 10 mL of saturatic sodium bicarbonate was added and the mixture concentrated in vacuo. Water (1000 mL) and ethyl acetate (1000 mL) were added to the solid residue, the pH was adjusted to 11, and the layers were separated. The organic phase was washed with water (2×), dried (sodium sulfate), filtered and evaporated. Recrystalization from ethyl acetate-hexane gave 14.5 g of [(7SR,9aSR)-2-(pyrimidin-2-yl)-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido[1,2-a]pyrazin-7-yl]acetonitrile. 13C NMR (CDCl3): d 19.5, 24.1, 26.9, 31.3, 33.1, 43.6, 48.9, 54.5, 109.8, 119.8, 157.7, 161.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220753B2
Source datasetuspto-grants-2007_05
ORD IDord-9a0c0f5c252a49388848bb81e469981c
Source noteuspto-grants-2007_05